JP2647696B2 - Surface modification method for plastic parts - Google Patents
Surface modification method for plastic partsInfo
- Publication number
- JP2647696B2 JP2647696B2 JP63208565A JP20856588A JP2647696B2 JP 2647696 B2 JP2647696 B2 JP 2647696B2 JP 63208565 A JP63208565 A JP 63208565A JP 20856588 A JP20856588 A JP 20856588A JP 2647696 B2 JP2647696 B2 JP 2647696B2
- Authority
- JP
- Japan
- Prior art keywords
- coating
- paint
- parts
- coating film
- plastic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/06—Polyurethanes from polyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/0427—Coating with only one layer of a composition containing a polymer binder
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/046—Forming abrasion-resistant coatings; Forming surface-hardening coatings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2475/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/904—Artificial leather
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31573—Next to addition polymer of ethylenically unsaturated monomer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31573—Next to addition polymer of ethylenically unsaturated monomer
- Y10T428/31583—Nitrile monomer type [polyacrylonitrile, etc.]
Description
【発明の詳細な説明】 (産業上の利用分野) この発明は、自動車車体に用いられているようなプラ
スチック部品の表面改質方法に関するものである。Description: TECHNICAL FIELD The present invention relates to a method for modifying the surface of a plastic component such as used in an automobile body.
(従来の技術) 従来のプラスチック部品の表面改質方法としては、次
のようなものがある。(Prior Art) Conventional methods for modifying the surface of plastic parts include the following.
(イ)従来塗装工法 プラスチック部品の表面にアクリルラッカーや塩素化
ポリオレフィン樹脂等を基体樹脂とする1液型塗料、又
は、アクリルポリオール樹脂を基体樹脂とする2液型ウ
レタン塗料を塗装する工法、 (ロ)塩化ビニル巻きつけ 樹脂基材に接着剤を塗布し、塩化ビニル表皮材を圧着
する工法。(A) Conventional coating method A method of applying a one-pack type paint using acrylic lacquer or chlorinated polyolefin resin or the like as a base resin or a two-pack type urethane paint using an acrylic polyol resin as a base resin on the surface of a plastic component, B) Winding vinyl chloride A method of applying an adhesive to the resin base material and pressing the vinyl chloride skin material.
(発明が解決しようとする課題) しかしながら、このような従来のプラスチック部品の
表面改質方法にあって、その塗装工法においては、硬質
基体樹脂を使用していたため、塗膜が硬くなり、ソフト
感が実現できない。また塩化ビニル巻きつけ工法におい
ては、接着精度が要求されるため、工程の歩留りが悪く
コストが上がるという問題点があった。(Problems to be Solved by the Invention) However, in such a conventional method for modifying the surface of a plastic part, in the coating method, a hard base resin is used, so that the coating film becomes hard and a soft feeling is obtained. Cannot be realized. Further, in the vinyl chloride winding method, there is a problem that since the bonding accuracy is required, the yield of the process is poor and the cost is increased.
(課題を解決するための手段) 本発明者等は従来のプラスチック部品の表示改質法の
解決すべき課題につき種々検討を行った結果、プラスチ
ック部品表面に20℃における伸び率60〜180%、摩擦係
数0.5〜0.8、初期弾性率60〜150kg/cm2の塗膜物性を有
する軟質系2液型ウレタン塗料を、20〜150μmの膜厚
で塗装することにより、プラスチック部品の表面の触感
がソフトになり、皮革に似た風合いが付与されることを
確かめ本発明を達成するに至った。(Means for Solving the Problems) As a result of various studies on the problems to be solved by the conventional display modification method for plastic parts, the present inventors have found that the elongation percentage at 20 ° C. coefficient of friction 0.5-0.8, a soft-based two-liquid type urethane paint having coating film properties of the initial elastic modulus 60~150kg / cm 2, by coating with a thickness of 20 to 150 [mu] m, software touch the surface of the plastic part It was confirmed that a texture similar to leather was imparted, and the present invention was achieved.
本発明のプラスチック部品の表示改質方法により表面
を改質するのに適用されるプラスチック部品としては、
アクリロニトリル・ブタジエン・スチレン共重合体(AB
S)樹脂、ポリプロピレン(PP)樹脂、PP複合材等から
成る自動車用のプラスチック部品の如き部品を例示する
ことができる。The plastic parts applied to modify the surface by the method for modifying the display of plastic parts of the present invention include:
Acrylonitrile-butadiene-styrene copolymer (AB
Parts such as S) resin, polypropylene (PP) resin, plastic parts for automobiles made of PP composite and the like can be exemplified.
(作 用) 次に作用を説明する。(Operation) Next, the operation will be described.
ここで「皮革の風合い」とは次の3つで表現できる: (イ)スベリ感→摩擦係数 (ロ)ヌメリ感→初期弾性率 (ハ)ソフト感→伸び率 すなわち、皮革に似た風合いを付与するためには、塗
膜の摩擦係数0.5〜0.8、初期弾性率60〜150kg/cm2、伸
び率60〜180%(20℃)の軟質系塗料を膜厚20〜150μm
で塗装することが有効である。摩擦係数が0.5より小さ
いとプラスチック感を生じ、0.8より大きいとゴム質感
となる。また、初期弾性率が150kg/cm2より大きい触感
が硬く、60kg/cm2より小さいと塗膜の強度不足となる。
伸び率が60%より小さいとソフト感がなくなり、180%
より大きいと粘着感が生じる。膜厚が20μm未満だとソ
フト感が得られなく、150μmを超えるとスプレー塗装
において時間を要すことやタレ、タマリ等の不具合を生
じやすくなり好ましくない。Here, the "texture of leather" can be expressed in three ways: (a) slipperiness → coefficient of friction (b) slimyness → initial elasticity (c) softness → elongation rate. To apply, a soft paint having a coefficient of friction of 0.5 to 0.8, an initial elastic modulus of 60 to 150 kg / cm 2 , and an elongation of 60 to 180% (20 ° C.) is applied to a thickness of 20 to 150 μm.
It is effective to paint with. If the friction coefficient is smaller than 0.5, a plastic feeling is produced, and if it is larger than 0.8, a rubber-like feeling is obtained. On the other hand, when the initial elastic modulus is higher than 150 kg / cm 2, the feel is hard, and when it is lower than 60 kg / cm 2 , the strength of the coating film is insufficient.
If the elongation is less than 60%, the soft feeling disappears and 180%
If it is larger, a sticky feeling is generated. If the film thickness is less than 20 μm, a soft feeling cannot be obtained, and if it exceeds 150 μm, it takes a long time in spray coating and disadvantages such as sagging and tearing tend to occur, which is not preferable.
本発明において用いられる軟質系塗料としては、密着
性、耐候性等の諸性能に優れたイソシアネート硬化の2
液ポリエステル系ウレタン塗料、特に2液型ポリエステ
ルポリオール系ウレタン塗料が最適である。塗膜の伸び
性、弾性に富んだ他の塗料樹脂系としては、メラミン硬
化型ポリエステル系、2液型アクリルウレタン系など考
えられるが、両者とも可とう性と諸性能のバランスが不
十分であり、特に前者は高温焼付けによる強制乾燥を必
要とするため、被塗物プラスチック素材の耐熱性の点で
制約を受けるという欠点がある。As the soft paint used in the present invention, isocyanate-cured 2 which is excellent in various properties such as adhesion and weather resistance.
A liquid polyester-based urethane coating, particularly a two-pack polyester polyol-based urethane coating is most suitable. Other paint resin systems that are rich in stretchability and elasticity of the coating film include melamine-curable polyesters and two-pack acrylic urethanes, but both have insufficient balance between flexibility and various properties. The former, in particular, requires forced drying by baking at a high temperature, and thus has a drawback that the heat resistance of the plastic material to be coated is restricted.
2液型ポリエステル系ウレタン塗料のポリエステルポ
リオールとしては、数平均分子量1000〜5000、水酸基価
60〜200の可とう性に優れたタイプが良い。即ち、数平
均分子量1000未満では塗膜が脆い傾向となり、5000を超
えると溶剤への溶解性が低下するため、スプレー作業性
(糸ひき、膜厚不足)の問題を生じる。又、水酸基価60
未満では塗膜の強靭性におとり、200を超えると塗膜が
硬くなり過ぎてソフトな触感が得られにくい。As the polyester polyol of the two-pack polyester urethane coating, the number average molecular weight is 1000 to 5000, and the hydroxyl value is
A type with excellent flexibility of 60 to 200 is good. That is, when the number average molecular weight is less than 1,000, the coating film tends to be brittle, and when the number average molecular weight exceeds 5,000, the solubility in a solvent is reduced, which causes a problem of spray workability (stringing, insufficient film thickness). Also, hydroxyl value 60
If it is less than 200, the toughness of the coating film is low. If it exceeds 200, the coating film is too hard to obtain a soft touch.
硬化剤としては、ヘキサメチレンジイソシアネート
(HMDI)系、イソホロンジイソシアネート(IPDI)系、
キシリレンジイソシアネート(XDI)系などの各種変性
ポリイソシアネートの使用が可能であるが、塗膜の伸び
性、弾性のほか、自動車用プラスチック部品のようなプ
ラスチック部品用塗料に要求される耐候性、付着性、耐
水性等の諸性能に優れたHMDI系ポリイソシアネートが好
適である。硬化剤の添加量はポリエステルポリオールの
水酸基とイソシアネート基の当量比(NCO基/OH基)が0.
5〜2.0の範囲が好ましい。即ち、当量比が0.5未満では
未反応の水酸基が多く残存するため、塗膜の硬化性、耐
久性に劣り、2.0を超えると過剰ポリイソシアネートの
副反応により、塗膜の可とう性、付着性が低下する。Hexamethylene diisocyanate (HMDI), isophorone diisocyanate (IPDI),
Various modified polyisocyanates such as xylylene diisocyanate (XDI) can be used, but in addition to the extensibility and elasticity of the coating, the weather resistance and adhesion required for coatings for plastic parts such as automotive plastic parts HMDI-based polyisocyanates having excellent properties such as water resistance and water resistance are suitable. The amount of the curing agent added is such that the equivalent ratio of the hydroxyl group to the isocyanate group of the polyester polyol (NCO group / OH group) is 0.
A range from 5 to 2.0 is preferred. That is, if the equivalent ratio is less than 0.5, a large amount of unreacted hydroxyl groups remains, and the curability and durability of the coating film are inferior.If the equivalent ratio exceeds 2.0, the side reaction of excess polyisocyanate causes the flexibility and adhesion of the coating film. Decrease.
(実施例) 次に本発明を実施例および比較例によって具体的に説
明する。尚、以下の部は重量基準である。(Examples) Next, the present invention will be specifically described with reference to Examples and Comparative Examples. The following parts are based on weight.
実施例1〜4 第1表に示す実施例1〜4の各配合に準じ、まず艶消
し剤を除く各配合組成物をペイントシェーカー(東洋精
機製)で2時間混練した後、艶消し剤を添加し高速ディ
スパーで約10分間撹拌したものを主剤とした。Examples 1 to 4 According to the respective formulations of Examples 1 to 4 shown in Table 1, each of the blended compositions except the matting agent was first kneaded for 2 hours with a paint shaker (manufactured by Toyo Seiki), and then the matting agent was removed. What was added and stirred for about 10 minutes with a high-speed disper was used as a main ingredient.
得られた主剤25部に対し、硬化剤としてポリイソシア
ネート樹脂ワニスのポリハードR(オリジン電気(株)
製、商品名、HMID系)10部、キシレンと酢酸ブチルの等
量混合溶剤を添加し、スプレー粘度をフォードカップ#
4(20℃)で20秒に調整し、実施例1〜4の塗料組成物
を得た。To 25 parts of the obtained base material, as a curing agent, a polyisocyanate resin varnish, Polyhard R (Origin Electric Co., Ltd.)
10 parts, mixed solvent of equal amount of xylene and butyl acetate, and spray viscosity of Ford cup #
The temperature was adjusted to 20 seconds at 4 (20 ° C.) to obtain the coating compositions of Examples 1 to 4.
次に実施例1〜3の塗料組成物については、夫々プラ
スチック素材(A)のABS素材(TRB、三菱レーヨン
(株)製、商品名)に次の手順で塗装した。Next, each of the coating compositions of Examples 1 to 3 was applied to an ABS material (TRB, manufactured by Mitsubishi Rayon Co., Ltd., trade name) as a plastic material (A) in the following procedure.
先ずABS素材をイソプロピルアルコールでワイピング
脱脂し、次いで各供試塗料組成物をエアースプレーにて
60μmの膜厚になるように塗布し、室温で10分間セッテ
ィングした後、80℃で40分間強制乾燥し試験片を作製し
た。First, the ABS material is wiped and degreased with isopropyl alcohol, and then each test paint composition is air-sprayed.
The composition was applied to a thickness of 60 μm, set at room temperature for 10 minutes, and then forcibly dried at 80 ° C. for 40 minutes to prepare a test piece.
また実施例4の塗料組成物については、プラスチック
素材(B)のPP素材(K−7030R、チッソ(株)製、商
品名)に次の手順で塗装した。The coating composition of Example 4 was applied to a PP material (K-7030R, manufactured by Chisso Corporation, trade name) as a plastic material (B) in the following procedure.
先ずプラスチック素材(B)のPP素材を1,1,1トリク
ロルエタン蒸気洗浄1分間行なった後、プライマーとし
てプラネットPPプライマーグレイK−3〔オリジン電気
(株)製、商品名、稀釈シンナープラネットシンナー#
301、稀釈率:塗料/シンナー=10/4、塗装粘度11秒
(フォードカップ#4、20℃)〕を10〜15μm塗布し、
室温で10分間セッティングした。次いで供試塗料をエア
ースプレーにて60μmの膜厚になるように塗布し、室温
で10分間セッティングした後、80℃で40分間強制乾燥
し、試験片を作製した。First, the PP material of the plastic material (B) was washed with 1,1,1 trichloroethane vapor for 1 minute, and then as a primer, Planet PP Primer Gray K-3 (trade name, manufactured by Origin Electric Co., Ltd., diluted thinner Planet Thinner #)
301, dilution ratio: paint / thinner = 10/4, coating viscosity 11 seconds (Ford cup # 4, 20 ° C.)]
Set at room temperature for 10 minutes. Next, the test paint was applied by air spray so as to have a film thickness of 60 μm, set at room temperature for 10 minutes, and then forcibly dried at 80 ° C. for 40 minutes to prepare a test piece.
第1表に示す各成分は次の通りである。 The components shown in Table 1 are as follows.
ポリエステルポリオール樹脂ワニスI:数平均分子量350
0、水酸基価100、酸価5の軟質ポリエステルポリオール
樹脂80部とトルエンとメチルイソブチルケトン(MIBK)
の等量混合溶剤20部から成る樹脂溶液。Polyester polyol resin varnish I: number average molecular weight 350
0, 80 parts of soft polyester polyol resin with hydroxyl value of 100 and acid value of 5, toluene and methyl isobutyl ketone (MIBK)
A resin solution consisting of 20 parts by weight of a mixed solvent.
ポリエステルポリオール樹脂ワニスII:数平均分子量200
0、水酸基価155、酸価7の軟質ポリエステルポリオール
樹脂80部とキシレンとメチルイソブチルケトンの等量混
合溶剤20部から成る樹脂溶剤。Polyester polyol resin varnish II: number average molecular weight 200
A resin solvent comprising 80 parts of a soft polyester polyol resin having a hydroxyl value of 155 and an acid value of 7, and 20 parts of a mixed solvent of equivalent amounts of xylene and methyl isobutyl ketone.
ポリエステルポリオール樹脂ワニスIII:数平均分子量25
00、水酸基価145、酸価2の軟質ポリエステルポリオー
ル樹脂80部と酢酸ブチル20部から成る樹脂溶液。Polyester polyol resin varnish III: number average molecular weight 25
A resin solution comprising 80 parts of a soft polyester polyol resin having a hydroxyl value of 145 and an acid value of 2 and 20 parts of butyl acetate.
二酸化チタン:CR−600(石原産業(株)製、商品名) カーボンブラック:MA−100(三菱化成(株)製、商品
名) 添加剤:DC−3(トーレシリコーン(株)製、商品名) 溶剤:トルエンとメチルイソブチルケトンの等量混合溶
剤 艶消し剤:サイロイド161(富士デビィソン化学(株)
製、商品名) 以上のようにして実施例1〜4の塗料組成物を塗布し
たプラスチック試験片につき塗膜性能を評価し、又下記
試験方法で物性を評価し、得た結果を第2表に記載す
る。Titanium dioxide: CR-600 (trade name, manufactured by Ishihara Sangyo Co., Ltd.) Carbon black: MA-100 (trade name, manufactured by Mitsubishi Kasei Co., Ltd.) Additive: DC-3 (trade name, manufactured by Toray Silicone Co., Ltd.) Solvent: Equivalent mixed solvent of toluene and methyl isobutyl ketone Matting agent: Syloid 161 (Fuji Devison Chemical Co., Ltd.)
As described above, the coating film performance was evaluated for the plastic test pieces to which the coating compositions of Examples 1 to 4 were applied, and the physical properties were evaluated by the following test methods. It describes in.
尚、伸び率、初期弾性率の塗膜物性試験はポリプロピ
レン素材テストピースに供試塗料を形成塗膜として約10
0μmとなるように塗布し、前記条件で強制乾燥した
後、塗膜に5mmの幅のナイフカットをいれてから剥離し
たものを試料とした。試験装置はテンシロンSTM型引張
試験機((株)オリエンテック製)で試料長6cm、引張
速度5mm/min、温度20℃とした。また、比較例3のアク
リルラッカーは塗膜が脆く試料作成が困難のため試験で
きなかった。In addition, the elongation and the initial elastic modulus of the coating film physical properties test was performed on a polypropylene test piece using the test paint as a coating film.
It was applied so as to have a thickness of 0 μm, and after being forcibly dried under the above conditions, a 5 mm-width knife cut was made on the coating film and then peeled off to obtain a sample. The test apparatus was a Tensilon STM type tensile tester (manufactured by Orientec Co., Ltd.) at a sample length of 6 cm, a tensile speed of 5 mm / min, and a temperature of 20 ° C. Further, the acrylic lacquer of Comparative Example 3 could not be tested because the coating film was brittle and it was difficult to prepare a sample.
摩擦係数は、上記塗装方法により得られた塗膜をKES
−FB4(カトーテック(株))で、荷重50g、加圧力10
g、試料移動速度0.1cm/secの条件で測定した 比較例1 塗料膜厚を15μmとした以外は実施例1と同様の方法
で行なった。The coefficient of friction was determined by KES
-With FB4 (Kato Tech Co., Ltd.), load 50g, pressure 10
g, measured under the conditions of a sample moving speed of 0.1 cm / sec. Comparative Example 1 The same procedure as in Example 1 was carried out except that the paint film thickness was changed to 15 μm.
比較例2 2液型アクリルウレタン系ABS用塗料のプラネットPZ
艶消しグレイ(オリジン電気(株)製、商品名)主剤40
部に対し、実施例1と同様の硬化剤10部、キシレンと酢
酸ブチルの等量混合溶剤を添加し、スプレー粘度をフォ
ードカップ#4(20℃)で14秒に調整し、比較例2の塗
料組成物を得た。次いでこの塗料組成物を実施例1と同
様にプラスチック素材(A)のABS素材に塗布し、塗膜
性能および物性を測定し、結果を第2表に示す。Comparative Example 2 Planet PZ, a two-pack acrylic urethane ABS paint
Matte Gray (Origin Electric Co., Ltd., trade name) 40
To 10 parts of the mixture, 10 parts of the same curing agent as in Example 1 and a mixed solvent of an equal amount of xylene and butyl acetate were added, and the spray viscosity was adjusted to 14 seconds with a Ford cup # 4 (20 ° C.). A coating composition was obtained. Next, this coating composition was applied to the ABS material of the plastic material (A) in the same manner as in Example 1, and the coating film performance and physical properties were measured. The results are shown in Table 2.
比較例3 1液型アクリルラッカー系ABS用塗料のプラネットAX
艶消しグレイ(オリジン電気(株)製、商品名)にキシ
レンと酢酸ブチルの等量混合溶剤を添加し、スプレー粘
度をフォードカップ#4(20℃)で12秒に調整し、比較
例3の塗装組成物を得た。この塗料組成物につき比較例
2と同様にして塗膜性能および物性を測定し、結果を第
2表に示す。Comparative Example 3 One-pack acrylic lacquer ABS paint, Planet AX
To a matte gray (trade name, manufactured by Origin Electric Co., Ltd.) was added a mixed solvent of an equal amount of xylene and butyl acetate, and the spray viscosity was adjusted to 12 seconds with a Ford cup # 4 (20 ° C.). A coating composition was obtained. The coating film performance and physical properties of this coating composition were measured in the same manner as in Comparative Example 2, and the results are shown in Table 2.
(発明の効果) 以上説明してきたように、本発明はプラスチック部品
の表面に伸び率60〜180%(20℃)、摩擦係数0.5〜0.
8、初期弾性率60〜150kg/cm2の塗膜物性を有する2液型
ウレタン塗料を膜厚20〜150μmに塗装するという構成
としたことにより、効率よくプラスチック部品表面を触
感がソフトで皮革に似た風合いを有するように改質でき
るという効果が得られる。 (Effects of the Invention) As described above, the present invention provides an elongation rate of 60 to 180% (20 ° C) and a friction coefficient of 0.5 to 0.
8. The two-component urethane paint with a coating property of 60 to 150 kg / cm 2 with an initial elastic modulus of 60 to 150 kg / cm2 is applied to a film thickness of 20 to 150 μm, so that the surface of plastic parts can be made soft and leather efficiently with a soft touch. The effect of being able to be modified to have a similar texture is obtained.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 遠山 貴 神奈川県横浜市神奈川区宝町2番地 日 産自動車株式会社内 (72)発明者 長尾 憲忠 東京都福生市南田園2―1612―815 (72)発明者 藤沢 実 埼玉県所沢市久米1965―1 ──────────────────────────────────────────────────続 き Continued on the front page (72) Inventor Takashi Toyama 2 Takaracho, Kanagawa-ku, Yokohama-shi, Kanagawa Nissan Motor Co., Ltd. Person Minoru Fujisawa 1965-1 Kume, Tokorozawa, Saitama
Claims (1)
び率60〜180%、摩擦係数0.5〜0.8、初期弾性率60〜150
kg/cm2の塗膜物性を有する2液型ウレタン塗料を膜厚20
〜150μmで塗装することによりプラスチック表面の触
感をソフトにし皮革に似た風合いを付与することを特徴
とするプラスチック部品の表面改質方法。An elongation at 20 ° C. of 60 to 180%, a friction coefficient of 0.5 to 0.8, and an initial elasticity of 60 to 150 on the surface of a plastic part.
A two-pack urethane paint with a coating film property of kg / cm 2 with a film thickness of 20
A method for modifying the surface of a plastic part, characterized in that the surface of the plastic part is softened by painting with a thickness of up to 150 μm to give a texture similar to leather.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63208565A JP2647696B2 (en) | 1988-08-23 | 1988-08-23 | Surface modification method for plastic parts |
US08/074,009 US6013364A (en) | 1988-08-23 | 1993-06-09 | Plastic article surface reforming method and plastic arrangement thereby |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63208565A JP2647696B2 (en) | 1988-08-23 | 1988-08-23 | Surface modification method for plastic parts |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0256280A JPH0256280A (en) | 1990-02-26 |
JP2647696B2 true JP2647696B2 (en) | 1997-08-27 |
Family
ID=16558289
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63208565A Expired - Lifetime JP2647696B2 (en) | 1988-08-23 | 1988-08-23 | Surface modification method for plastic parts |
Country Status (2)
Country | Link |
---|---|
US (1) | US6013364A (en) |
JP (1) | JP2647696B2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2815295B2 (en) * | 1993-10-22 | 1998-10-27 | 日立造船株式会社 | Ocean input ship |
TW526304B (en) * | 1999-03-30 | 2003-04-01 | Kuraray Co | Process for producing a leather-like sheet |
JP2003317569A (en) * | 2002-04-18 | 2003-11-07 | Toyo Denso Co Ltd | Soft feel operation switch |
DE102007059090A1 (en) | 2007-12-07 | 2009-06-10 | Benecke-Kaliko Ag | polymer mixture |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3836423A (en) * | 1971-09-09 | 1974-09-17 | Hooker Chemical Corp | Method of introducing air permeability into a non-porous continuous film and resultant film |
JPS5221563B2 (en) * | 1973-07-04 | 1977-06-11 | ||
DE2801817C3 (en) * | 1978-01-17 | 1980-12-18 | Bayer Ag, 5090 Leverkusen | Pigment preparations |
DE3010719A1 (en) * | 1980-03-20 | 1981-09-24 | Bayer Ag, 5090 Leverkusen | METHOD FOR PRODUCING METAL EFFECT PAINTINGS AND WEATHER-RESISTANT METAL EFFECT MULTI-LAYER PAINT PAINTINGS |
JPS5949961A (en) * | 1982-09-16 | 1984-03-22 | 豊田合成株式会社 | Metallic brilliancy-like colored resin product |
DE3421122A1 (en) * | 1984-06-07 | 1985-12-12 | Bayer Ag, 5090 Leverkusen | NEW POLYESTER POLYOLS AND THEIR USE AS POLYOL COMPONENTS IN TWO-COMPONENT PLYURETHANE PAINTS |
US5061517A (en) * | 1989-11-22 | 1991-10-29 | Speer Lawrence L | Brush-on finish for footwear and similar articles |
-
1988
- 1988-08-23 JP JP63208565A patent/JP2647696B2/en not_active Expired - Lifetime
-
1993
- 1993-06-09 US US08/074,009 patent/US6013364A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH0256280A (en) | 1990-02-26 |
US6013364A (en) | 2000-01-11 |
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